FDA.reportPublic FDA data

Metoprolol Tartate

Product NDC
51655-535
11-digit product format
516550535
Labeler code
51655
Product ID
51655-535_fb98ff8e-3de0-4300-b6c7-5401d5856239
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Tartate
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Pharmaceuticals
Application
ANDA074644
Marketing category
ANDA
Marketing start
2014-06-02
Marketing end
0000-00-00
Substance
METOPROLOL TARTRATE
Active strength
50 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51655-535-252026-01-08C16284748780-19d75b9d0-2d3d-f424-e053-dadaa90a57ce760c63bd-1c1c-4a89-9f02-48aadb750484
51655-535-262026-01-08C16284748780-19d75b9d0-2d3d-f424-e053-dadaa90a57ce760c63bd-1c1c-4a89-9f02-48aadb750484
51655-535-522026-01-08C16284748780-19d75b9d0-2d3d-f424-e053-dadaa90a57ce760c63bd-1c1c-4a89-9f02-48aadb750484
51655-535-252020-01-31C16284748780-19d75b9d0-2d3d-f424-e053-dadaa90a57ce760c63bd-1c1c-4a89-9f02-48aadb750484
51655-535-262020-01-31C16284748780-19d75b9d0-2d3d-f424-e053-dadaa90a57ce760c63bd-1c1c-4a89-9f02-48aadb750484
51655-535-522020-01-31C16284748780-19d75b9d0-2d3d-f424-e053-dadaa90a57ce760c63bd-1c1c-4a89-9f02-48aadb750484

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
METOPROLOL TARTRATEACTIVE INGREDIENTW5S57Y3A5LMETOPROLOL TARTATE TABLET [NORTHWIND PHARMACEUTICALS]3
METOPROLOLACTIVE MOIETYGEB06NHM23METOPROLOL TARTATE TABLET [NORTHWIND PHARMACEUTICALS]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-535METOPROLOL TARTATE TABLET [NORTHWIND PHARMACEUTICALS]3Legacy NDC20150402_760c63bd-1c1c-4a89-9f02-48aadb750484.zip